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product_txtF_mv:"National Center for Biotechnology Information"
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1
Quality of reporting in systematic reviews of implantable medical devices
by
Raman, Gowri
Published 2012
Agency for Healthcare Research and Quality
Subjects:
“
...
Product
Surveillance
,
Postmarketing
...
”
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2
Ethical issues in studying the safety of approved drugs : a letter report
Published 2010
National Academies Press
Subjects:
“
...
Product
Surveillance
,
Postmarketing
...
”
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3
Ethical issues in studying the safety of approved drugs : a letter report
Published 2010
National Academies Press
Subjects:
“
...
Product
Surveillance
,
Postmarketing
...
”
Read Now
4
Dietary supplements : a framework for evaluating safety
Published 2005
The National Academies Press
Subjects:
“
...
Product
Surveillance
,
Postmarketing
/ methods...
”
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5
Challenges for the FDA : the future of drug safety : workshop summary
by
Pray, Leslie A.
Published 2007
National Academies Press
Subjects:
“
...
Product
Surveillance
,
Postmarketing
...
”
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6
Public health effectiveness of the FDA 510(k) clearance process : measuring postmarket performance and other select topics : workshop report
by
Wizemann, Theresa M.
Published 2011
National Academies Press
Subjects:
“
...
Product
Surveillance
,
Postmarketing
/ methods...
”
Call Number:
RA399.A3
Read Now
7
Ethical and scientific issues in studying the safety of approved drugs
Published 2012
National Academies Press
Subjects:
“
...
Product
Surveillance
,
Postmarketing
/ methods...
”
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658 - General management
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7
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National Center for Biotechnology Information
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Institute of Medicine (U.S.) Committee on Ethical and Scientific Issues in Studying the Safety of Approved Drugs
3
Committee on the Framework for Evaluating the Safety of Dietary Supplements
1
Institute of Medicine (U.S.) Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process
1
Institute of Medicine (U.S.) Forum on Drug Discovery, Development, and Translation
1
Pray, Leslie A.
1
Raman, Gowri
1
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Robinson, Sally
1
Symposium on the Future of Drug Safety: Challenges for the FDA (2007, Washington, D.C.)
1
Tufts Evidence-based Practice Center
1
United States Agency for Healthcare Research and Quality
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Wizemann, Theresa M.
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